Source:http://linkedlifedata.com/resource/pubmed/id/18057010
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2008-2-18
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pubmed:abstractText |
E-cadherins play an essential role in maintaining epithelial polarity by forming Ca2+-dependent adherens junctions between epithelial cells. Here, we report that Ca2+ depletion induces E-cadherin ubiquitination and lysosomal degradation and that Cdc42 plays an important role in regulating this process. We demonstrate that Ca2+ depletion induces activation of Cdc42. This in turn up-regulates epidermal growth factor receptor (EGFR) signaling to mediate Src activation, leading to E-cadherin ubiquitination and lysosomal degradation. Silencing Cdc42 blocks activation of EGFR and Src induced by Ca2+ depletion, resulting in a reduction in E-cadherin degradation. The role of Cdc42 in regulating E-cadherin ubiquitination and degradation is underscored by the fact that constitutively active Cdc42(F28L) increases the activity of EGFR and Src and significantly enhances E-cadherin ubiquitination and lysosomal degradation. Furthermore, we found that GTP-dependent binding of Cdc42 to E-cadherin is critical for Cdc42 to induce the dissolution of adherens junctions. Our data support a model that activation of Cdc42 contributes to mesenchyme-like phenotype by targeting of E-cadherin for lysosomal degradation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cadherins,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins pp60(c-src),
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Fibroblast Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin,
http://linkedlifedata.com/resource/pubmed/chemical/cdc42 GTP-Binding Protein
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
283
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5127-37
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:18057010-Adherens Junctions,
pubmed-meshheading:18057010-Amino Acid Substitution,
pubmed-meshheading:18057010-Cadherins,
pubmed-meshheading:18057010-Calcium,
pubmed-meshheading:18057010-Cell Line,
pubmed-meshheading:18057010-Enzyme Activation,
pubmed-meshheading:18057010-Epithelial Cells,
pubmed-meshheading:18057010-Gene Silencing,
pubmed-meshheading:18057010-Humans,
pubmed-meshheading:18057010-Lysosomes,
pubmed-meshheading:18057010-Mutation, Missense,
pubmed-meshheading:18057010-Proto-Oncogene Proteins pp60(c-src),
pubmed-meshheading:18057010-Receptors, Fibroblast Growth Factor,
pubmed-meshheading:18057010-Signal Transduction,
pubmed-meshheading:18057010-Ubiquitin,
pubmed-meshheading:18057010-Ubiquitination,
pubmed-meshheading:18057010-cdc42 GTP-Binding Protein
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pubmed:year |
2008
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pubmed:articleTitle |
Cdc42 regulates E-cadherin ubiquitination and degradation through an epidermal growth factor receptor to Src-mediated pathway.
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pubmed:affiliation |
Division of Monoclonal Antibodies, Office of Biotechnology Products, Center for Drug Evaluation and Research, United States Food and Drug Administration, Bethesda, Maryland 20892-4555, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
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